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Deutan defect

disorder
SNOMED 77479002CUI C3887938

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Deuteranomaly
HP:0011520

Quick Facts

SNOMED CT
77479002
UMLS CUI
C3887938
Fully Specified Name
Deutan defect (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
1
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.